Endoshape, Inc. is one of 5101 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Endoshape, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Endoshape, Inc. has 2 FDA 510(k) cleared medical devices. Based in Boulder, US.
Historical record: 2 cleared submissions from 2013 to 2014. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Endoshape, Inc. Filter by specialty or product code using the sidebar.
Endoshape, Inc. — FDA 510(k) Products and Clearance History
2 devices
Cleared
Dec 02, 2014
MEDUSA VASCULAR PLUG,
Cardiovascular
246d
Cleared
Oct 25, 2013
MEDUSA VASCULAR PLUG
Cardiovascular
326d